Neural Correlates of Motor Imagery of Gait in Amyotrophic Lateral Sclerosis

被引:50
作者
Abidi, Malek [1 ]
de Marco, Giovanni [1 ,2 ]
Grami, Fatma [1 ]
Termoz, Nicolas [1 ,2 ]
Couillandre, Annabelle [1 ,2 ]
Querin, Giorgia [3 ,4 ]
Bede, Peter [3 ,4 ,5 ]
Pradat, Pierre-Francois [3 ,4 ,6 ]
机构
[1] Paris Nanterre Univ, AAPS Lab, LINP2, UPL, Nanterre, France
[2] COMUE Paris Lumieres Univ, Paris, France
[3] Pitie Salpetriere Univ Hosp, Dept Neurol, Paris, France
[4] Sorbonne Univ, Biomed Imaging Lab, CNRS, INSERM, Paris, France
[5] Trinity Coll Dublin, Computat Neuroimaging Grp, Dublin, Ireland
[6] Ulster Univ, Biomed Sci Res Inst, Northern Ireland Ctr Stratified Med, Londonderry, North Ireland
关键词
ALS; INVOLVEMENT; DYSFUNCTION; VALIDATION; FEATURES; CRITERIA;
D O I
10.1002/jmri.27335
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background Gait impairment is poorly characterized in amyotrophic lateral sclerosis (ALS), despite increasing evidence of extrapyramidal and cerebellar dysfunction. Gait impairment adds to the considerable motor disability of ALS patients and requires targeted multidisciplinary interventions. Purpose To assess gait imagery-specific networks and functional adaptation in ALS. Study Type Prospective. Population SeventeenALSpatients with lower motor neuron predominant (LMNp) disability, 14 patients with upper motor neurons predominant (UMNp) disease, and 14 healthy controls were included. Field Strength/Sequences 3T / gradient echo echo planar (GE-EPI). Assessment Subjects performed a dual motor imagery task: normal and precision gait. The Movement Imagery Questionnaire - Revised Second Version (MIQ-rs) was used to appraise movement imagery in each participant. Study group-specific activation patterns were evaluated during motor imagery of gait. Additional generalized psychophysiological interaction analyses were carried out using the supplementary motor area, caudate, cerebellum, and superior parietal lobule as seed regions. Statistical Tests Repeated-measures analysis of variance (ANOVA) was used to compare time imagery and MIQ-rs scores between groups. Size effects were also reported as partial eta squared (eta 2). One-way ANOVA was performed to explore differences in terms of connexions during motor imagery tasks. Results A significant increase in imagery time in UMNp patients compared to controls (P < 0.05) and LMNp (P < 0.05) during imagined gait was demonstrated. UMNp patients exhibited altered supplementary motor area, precentral gyrus, superior parietal lobule, and dorsolateral prefrontal cortex activation and increased orbitofrontal (pFDR((False Discovery Rate)) < 0.05), posterior parietal (pFDR < 0.05) caudate (pFDR < 0.05), and cerebellar (pFDR < 0.05) signal during imagined locomotion. Increased effective connectivity of the striato-cerebellar and parieto-cerebellar circuits was also demonstrated. Additional activation was detected in the insula and cingulate cortex. Data Conclusion Enhanced striato- and parieto-cerebellar networks in UMNp ALS patients are likely to represent a compensatory response to impaired postural control. Level of Evidence 2 Technical Efficacy Stage 5
引用
收藏
页码:223 / 233
页数:11
相关论文
共 40 条
[1]   What disconnection tells about motor imagery: Evidence from paraplegic patients [J].
Alkadhi, H ;
Brugger, P ;
Boendermaker, SH ;
Crelier, G ;
Curt, A ;
Hepp-Reymond, MC ;
Kollias, SS .
CEREBRAL CORTEX, 2005, 15 (02) :131-140
[2]   Cerebral correlates of motor imagery of normal and precision gait [J].
Bakker, M. ;
De Lange, F. P. ;
Helmich, R. C. ;
Scheeringa, R. ;
Bloem, B. R. ;
Toni, I. .
NEUROIMAGE, 2008, 41 (03) :998-1010
[3]   Patterns of cerebral and cerebellar white matter degeneration in ALS [J].
Bede, P. ;
Elamin, M. ;
Byrne, S. ;
McLaughlin, R. L. ;
Kenna, K. ;
Vajda, A. ;
Fagan, A. ;
Bradley, D. G. ;
Hardiman, O. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2015, 86 (04) :468-+
[4]   Connectivity-based characterisation of subcortical grey matter pathology in frontotemporal dementia and ALS: a multimodal neuroimaging study [J].
Bede, Peter ;
Omer, Taha ;
Finegan, Eoin ;
Chipika, Rangariroyashe H. ;
Iyer, Parameswaran M. ;
Doherty, Mark A. ;
Vajda, Alice ;
Pender, Niall ;
McLaughlin, Russell L. ;
Hutchinson, Siobhan ;
Hardiman, Orla .
BRAIN IMAGING AND BEHAVIOR, 2018, 12 (06) :1696-1707
[5]   Action prediction in the cerebellum and in the parietal lobe [J].
Blakemore, SJ ;
Sirigu, A .
EXPERIMENTAL BRAIN RESEARCH, 2003, 153 (02) :239-245
[6]   El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis [J].
Brooks, BR ;
Miller, RG ;
Swash, M ;
Munsat, TL .
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS, 2000, 1 (05) :293-299
[7]   Measurement of Social Cognition in Amyotrophic Lateral Sclerosis: A Population Based Study [J].
Burke, Tom ;
Pinto-Grau, Marta ;
Lonergan, Katie ;
Elamin, Marwa ;
Bede, Peter ;
Costello, Emmet ;
Hardiman, Orla ;
Pender, Niall .
PLOS ONE, 2016, 11 (08)
[8]   The precuneus: a review of its functional anatomy and behavioural correlates [J].
Cavanna, AE ;
Trimble, MR .
BRAIN, 2006, 129 :564-583
[9]   The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function [J].
Cedarbaum, JM ;
Stambler, N ;
Malta, E ;
Fuller, C ;
Hilt, D ;
Thurmond, B ;
Nakanishi, A .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 169 (1-2) :13-21
[10]   Tracking a Fast-Moving Disease: Longitudinal Markers, Monitoring, and Clinical Trial Endpoints in ALS [J].
Chipika, Rangariroyashe Hannah ;
Finegan, Eoin ;
Shing, Stacey Li Hi ;
Hardiman, Orla ;
Bede, Peter .
FRONTIERS IN NEUROLOGY, 2019, 10